Allele Registry

Canonical Allele Identifier: PA2825438449

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001367751

ClinVar Variation:

1058594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070651.1:p.Gly1376Val	CA394301384 NM_001077183.3:c.4127G>T